Indianapolis, IN, United States · Est. 1876 · 43,000 employees
Global healthcare leader creating medicines that make life better.
Pipeline Programs↗
Distinct drugs in development (Preclinical–Phase 3)
Indications↗
Distinct diseases across all programs
Clinical Trials↗
All sponsored trials (all statuses)
Orange Book Patents
Across 9 drugs with upcoming expirations
Pipeline
By Phase
89 drugs in development
By Therapeutic Area
top 6
R&D Momentum
100/100
Pipeline Velocity
85/100
Trial Completion Rate
92/100
Pipeline Concentration
13/100
Pipeline Freshness
74/100
Strategic Signals
Activity
Last 14 days
A Phase 2, Randomized, Open-Label, Comparator-Controlled Trial to Evaluate the Efficacy and Safety of LY3938577 in Study Participants, With Type 2 Diabetes Previously Treated With Basal Insulin
An Open Label, Randomized, Single Dose, 2-Way Crossover Study to Evaluate the Pharmacokinetics of Pre-filled Syringe Versus Vial Formulations of AM0010 in Healthy Adult Subjects
FORAGER-2: A Phase 3, Randomized, Double-blind, Placebo-controlled Study Evaluating the Efficacy and Safety of Vepugratinib Combined With Enfortumab Vedotin and Pembrolizumab in Adults With Untreated Locally Advanced or Metastatic Urothelial Carcinoma With an FGFR3 Genetic Alteration
An Open-label, Dose-Finding, Phase 1/2 Study to Evaluate the Safety and Tolerability of a Single Intravenous Dose of LY3884961 in Patients With Peripheral Manifestations of Gaucher Disease (PROCEED)
A Randomized, Controlled Pragmatic Phase 3b/4 Study of Baricitinib in Patients With Rheumatoid Arthritis
A Single- and Multiple-Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3502970 in Healthy Subjects
A Phase 2, Randomized, Double-Blind, Placebo Controlled, Dose-Finding Study Evaluating LY3848575 in Chronic Neuropathic Pain Associated With Distal Sensory Polyneuropathy
A Multiple Dose Study to Assess the Pharmacokinetics, Safety, and Tolerability of Tablet and Capsule Formulations of LY3502970 in Healthy Overweight and Obese Participants
BAF_FRontier-1, A First-in-Human, Phase 1 Trial to Assess Safety, Tolerability, and Preliminary Efficacy of LY4152199, a B-cell Activation Factor Receptor (BAFF-R) T-Cell Engager Bispecific Antibody in Adult Participants With Previously Treated B-cell Malignancies
A Phase 1, Open-Label Dose Escalation First-in-Human Study to Evaluate the Tolerability, Safety, Maximum Tolerated Dose, Preliminary Clinical Activity and Pharmacokinetics of AM0010 in Patients With Advanced Solid Tumors
A Phase 1 Study of LY3410738 Administered to Patients With Advanced Solid Tumors With IDH1 or IDH2 Mutations
Details
Company Overview
$750.0B
Mkt Cap
$34.1B
Revenue
$3.6B
Cash
Therapeutic Focus
Pipeline
Regulatory
Taltz — TALTZ
Application BLA125521 (BLA)
Humalog — ADMELOG
Application BLA209196 (BLA)
Verzenio — VERZENIO
Application NDA208716 (NDA)
Emgality — EMGALITY
Application BLA761063 (BLA)
Olumiant — OLUMIANT
Application NDA207924 (NDA)
LYUMJEV — LYUMJEV
Application BLA761109 (BLA)
Retevmo — RETEVMO
Application NDA213246 (NDA)
Reyvow — REYVOW
Application NDA211280 (NDA)
Cialis — TADLIQ
Application NDA214522 (NDA)
Omvoh — OMVOH
Application BLA761279 (BLA)
Mounjaro — MOUNJARO
Application NDA215866 (NDA)
Jaypirca — JAYPIRCA
Application NDA216059 (NDA)
EBGLYSS — EBGLYSS
Application BLA761306 (BLA)
Kisunla — KISUNLA
Application BLA761248 (BLA)
Cialis — CHEWTADZY
Application NDA218527 (NDA)
Retevmo — RETEVMO
Application NDA218160 (NDA)
Mounjaro — ZEPBOUND
Application NDA217806 (NDA)
Inluriyo — INLURIYO
Application NDA218881 (NDA)
Foundayo — FOUNDAYO
Application NDA220934 (NDA)
Folvite — QUIOFIC
Application NDA216395 (NDA)
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)